Hu Ying-Yue, Wang Yun-Can, Qin Wen-Xiu, Yu Shuo, Dai Si-Yang, Pei Yue-Hu, Li Chang, Yang Yi-Hui
Department of Medicinal Chemistry and Natural Medicine Chemistry, College of Pharmacy, Harbin Medical University, Harbin 150081, PR China.
Curr Pharm Des. 2025;31(30):2438-2463. doi: 10.2174/0113816128365838250128060007.
Psoralen, the simplest linear furanocoumarin, is derived from many medicinal plants, such as L., Fr. Schmidt ex Miq., and Peucedanum decursivum (Miq.) Maxim. It has been used for treating osteoporosis and some skin disorders, including vitiligo, psoriasis, and atopic eczema. This review focuses on the pharmaceutical design of psoralen and the structure-activity relationships (SARs) of its derivatives. It also includes the biosynthetic pathways, metabolic characteristics, metabolites, and clinical uses of psoralen, as well as its toxicity/side effects and relevant mechanisms. Psoralen, as a promising drug lead compound, is structurally modified to develop numerous derivatives with remarkable biological activities. SARs discussed herein can guide the design and development of novel psoralen-based derivatives for use in pharmaceuticals and widen their therapeutic potencies.
补骨脂素是最简单的线性呋喃香豆素,它源自多种药用植物,如光果甘草、兴安白芷和紫花前胡。它已被用于治疗骨质疏松症和一些皮肤疾病,包括白癜风、银屑病和特应性皮炎。本综述重点关注补骨脂素的药物设计及其衍生物的构效关系(SARs)。它还包括补骨脂素的生物合成途径、代谢特征、代谢产物和临床用途,以及其毒性/副作用和相关机制。补骨脂素作为一种有前景的药物先导化合物,在结构上进行修饰以开发出许多具有显著生物活性的衍生物。本文讨论的构效关系可以指导新型补骨脂素基衍生物的设计和开发,用于制药领域,并扩大其治疗效力。